Ka Cheuk Liu

Mechanistic insights and approaches for beta cell regeneration

Karampelias, Christos; Liu, Ka-Cheuk; Tengholm, Anders; Andersson, Olov

Ingår i Nature Chemical Biology, 2025

• DOI för Mechanistic insights and approaches for beta cell regeneration

Excess pancreatic elastase alters acinar-β cell communication by impairing the mechano-signaling and the PAR2 pathways

Basile, Giorgio; Vetere, Amedeo; Hu, Jiang; Ijaduola, Oluwaseun et al.

Ingår i Cell Metabolism, s. 1242-1260000000000, 2023

• DOI för Excess pancreatic elastase alters acinar-β cell communication by impairing the mechano-signaling and the PAR2 pathways

Decoding pancreatic endocrine cell differentiation and β cell regeneration in zebrafish

Mi, Jiarui; Liu, Ka‐Cheuk; Andersson, Olov

Ingår i Science Advances, 2023

• DOI för Decoding pancreatic endocrine cell differentiation and β cell regeneration in zebrafish

In vivo drug discovery for increasing incretin-expressing cells identifies DYRK inhibitors that reinforce the enteroendocrine system

Chu, Lianhe; Terasaki, Michishige; Mattsson, Charlotte L.; Teinturier, Romain et al.

Ingår i Cell Chemical Biology, s. 1368-138000000, 2022

• DOI för In vivo drug discovery for increasing incretin-expressing cells identifies DYRK inhibitors that reinforce the enteroendocrine system

Insulin-producing β-cells regenerate ectopically from a mesodermal origin under the perturbation of hemato-endothelial specification

Liu, Ka‐Cheuk; Villasenor, Alethia; Bertuzzi, Maria; Schmitner, Nicole et al.

Ingår i eLIFE, 2021

• DOI för Insulin-producing β-cells regenerate ectopically from a mesodermal origin under the perturbation of hemato-endothelial specification

Mechanistic insights and approaches for beta cell regeneration

Karampelias, Christos; Liu, Ka-Cheuk; Tengholm, Anders; Andersson, Olov

Ingår i Nature Chemical Biology, 2025

• DOI för Mechanistic insights and approaches for beta cell regeneration

Excess pancreatic elastase alters acinar-β cell communication by impairing the mechano-signaling and the PAR2 pathways

Basile, Giorgio; Vetere, Amedeo; Hu, Jiang; Ijaduola, Oluwaseun et al.

Ingår i Cell Metabolism, s. 1242-1260000000000, 2023

• DOI för Excess pancreatic elastase alters acinar-β cell communication by impairing the mechano-signaling and the PAR2 pathways

Decoding pancreatic endocrine cell differentiation and β cell regeneration in zebrafish

Mi, Jiarui; Liu, Ka‐Cheuk; Andersson, Olov

Ingår i Science Advances, 2023

• DOI för Decoding pancreatic endocrine cell differentiation and β cell regeneration in zebrafish

In vivo drug discovery for increasing incretin-expressing cells identifies DYRK inhibitors that reinforce the enteroendocrine system

Chu, Lianhe; Terasaki, Michishige; Mattsson, Charlotte L.; Teinturier, Romain et al.

Ingår i Cell Chemical Biology, s. 1368-138000000, 2022

• DOI för In vivo drug discovery for increasing incretin-expressing cells identifies DYRK inhibitors that reinforce the enteroendocrine system

Insulin-producing β-cells regenerate ectopically from a mesodermal origin under the perturbation of hemato-endothelial specification

Liu, Ka‐Cheuk; Villasenor, Alethia; Bertuzzi, Maria; Schmitner, Nicole et al.

Ingår i eLIFE, 2021

• DOI för Insulin-producing β-cells regenerate ectopically from a mesodermal origin under the perturbation of hemato-endothelial specification

Spatiotemporal expression analysis of nuclear estrogen receptors in the zebrafish ovary and their regulation in vitro by endocrine hormones and paracrine factors

Liu, Ka-Cheuk; Lau, Shuk-Wa; Ge, Wei

Ingår i General and Comparative Endocrinology, s. 218-225, 2017

• DOI för Spatiotemporal expression analysis of nuclear estrogen receptors in the zebrafish ovary and their regulation in vitro by endocrine hormones and paracrine factors

Inhibition of Cdk5 Promotes β-Cell Differentiation From Ductal Progenitors

Liu, Ka‐Cheuk; Leuckx, Gunter; Sakano, Daisuke; Seymour, Philip A. et al.

Ingår i Diabetes, s. 58-70, 2017

• DOI för Inhibition of Cdk5 Promotes β-Cell Differentiation From Ductal Progenitors

IGFBP1 increases β‐cell regeneration by promoting α‐ to β‐cell transdifferentiation

Lu, Jing; Liu, Ka‐Cheuk; Schulz, Nadja; Karampelias, Christos et al.

Ingår i EMBO Journal, s. 2026-2044, 2016

• DOI för IGFBP1 increases β‐cell regeneration by promoting α‐ to β‐cell transdifferentiation

Critical role for adenosine receptor A2a in β-cell proliferation

Schulz, Nadja; Liu, Ka-Cheuk; Charbord, Jérémie; Mattsson, Charlotte L. et al.

Ingår i Molecular Metabolism, s. 1138-1146, 2016

• DOI för Critical role for adenosine receptor A2a in β-cell proliferation

Differential regulation of gonadotropin receptors (fshr and lhcgr) by epidermal growth factor (EGF) in the zebrafish ovary

Liu, Ka-Cheuk; Ge, Wei

Ingår i General and Comparative Endocrinology, s. 288-294, 2013

• DOI för Differential regulation of gonadotropin receptors (fshr and lhcgr) by epidermal growth factor (EGF) in the zebrafish ovary

Evidence for Gating Roles of Protein Kinase A and Protein Kinase C in Estradiol-Induced Luteinizing Hormone Receptor (lhcgr) Expression in Zebrafish Ovarian Follicle Cells

Liu, Ka-Cheuk; Ge, Wei

Ingår i PLOS ONE, 2013

• DOI för Evidence for Gating Roles of Protein Kinase A and Protein Kinase C in Estradiol-Induced Luteinizing Hormone Receptor (lhcgr) Expression in Zebrafish Ovarian Follicle Cells

Luteinizing hormone receptor (lhcgr) as a marker gene for characterizing estrogenic endocrine-disrupting chemicals in zebrafish ovarian follicle cells

Liu, Ka-Cheuk; Wu, Rudolf S.S.; Ge, Wei

Ingår i General and Comparative Endocrinology, s. 89-94, 2013

• DOI för Luteinizing hormone receptor (lhcgr) as a marker gene for characterizing estrogenic endocrine-disrupting chemicals in zebrafish ovarian follicle cells

Differential Regulation of Gonadotropin Receptors (fshr and lhcgr) by Estradiol in the Zebrafish Ovary Involves Nuclear Estrogen Receptors That Are Likely Located on the Plasma Membrane

Liu, Ka-Cheuk; Lin, Sze-Wah; Ge, Wei

Ingår i Endocrinology, s. 4418-4430, 2011

• DOI för Differential Regulation of Gonadotropin Receptors (fshr and lhcgr) by Estradiol in the Zebrafish Ovary Involves Nuclear Estrogen Receptors That Are Likely Located on the Plasma Membrane